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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Бондарь В.С., Высоцкий Е.С., Гамалей И.А., Каулин А.Б.
Заглавие : Получение, свойства и применение кальцийчувствительного фотопротеина из гидроида Obelia longissima : научное издание
Место публикации : Цитология. - 1991. - Т. 33, N 6. - С. 50-59. - ISSN 0041-3771
ГРНТИ : 31.23.27
Предметные рубрики: ФОСФОПРОТЕИНЫ
КАЛЬЦИЙ ЧУВСТВИТЕЛЬНЫЙ
ВЫДЕЛЕНИЕ
ГИДРОЛИЗ
OBELIA LONGISSIMA
OBELIN
PHOSPHOMOTEIN
CHROMATOGRAPHY
Аннотация: С помощью Ca{2}{+} - активируемого протеина белина измеряли конц-ию свободного ионизированного кальция в макрофагах (МФ) в покое и при действии различных стимуляторов. Использовали обелин, выделенный из гидроида Obelia longissima и очищенный с использованием гельфильтрации на Сефадексе, ИОХ на полисиле, гидрофобной хр-фии на фенил-сефарозе, повторной гель-фильтрации на Сефадексе. Нагрузку МФ фотопротеином проводили модифицированным методом "осмотического лизиса пиносом". Фоновое значение конц-ии цитоплазматич. кальция [Ca{2}{+}][j] в покоящихся МФ, зарегистрированное с помощью обелина, соответствует 0,5-0,7 мкМ. Сыворотка крупного рогатого скота (20%) стимулирует периодич. импульсное повышение [Ca{2}{+}][j] до 1,3 мкМ с быстрым падением практически до уровня фона, наблюдаемое в течение не менее 30 мин, NaF (20 мМ), добавленный к суспензии МФ, вызывает быстрое однократное увеличение [Ca{2}{+}][j] до 1,4 мкМ. АТФ (30-60 мкМ) стимулирует повышение [Ca{2}{+}][j] в МФ до 1,5 мкМ. цАМФ (20 мкМ) повышает конц-ию свободного внутриклеточного кальция до 1,5 мкМ с быстрым падением и возвращением за 30 с к уровню фона, при этом ЭГТА (2 мМ) не снимает стимулирующего эффекта цАМФ на МФ. При изменении внутриклеточного рН МФ в щелочную сторону эффект цАМФ качественно сохраняется, однако повышение [Ca{2}{+}][j] менее выражено. Закисление цитоплазмы вызывает качественное и количеств. изменение кальциевого ответа МФ на добавку цАМФ: [Ca{2}{+}][j] не повышается более чем до 1,3 мкМ, время достижения макс. уровня [Ca{2}{+}][j] и возвращения к исходному фону увеличено. Рассматриваются возможные мех-мы действия различных стимуляторов на МФ, сопровождающиеся повышением уровня внутриклеточного свободного кальция. Библ. 38. Россия, Ин-т биофизики СОРАН, Красноярск.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Frank L.A., Illarionova V.A., Vysotski E.S.
Заглавие : Use of proZZ-obelin fusion protein in bioluminescent immunoassay
Место публикации : Biochem. Biophys. Res. Commun.: ACADEMIC PRESS INC JNL-COMP SUBSCRIPTIONS, 1996. - Vol. 219, Is. 2. - С. 475-479. - 5. - ISSN 0006-291X, DOI 10.1006/bbrc.1996.0258
Примечания : Cited References: 21
Предметные рубрики: ESCHERICHIA-COLI
EXPRESSION
AEQUORIN
PURIFICATION
SYSTEM
Аннотация: Obelin is a photoprotein that emits light by Ca2+-binding. To develop a bioluminescent immunoassay based on the light emission property of obelin, we have expressed the apoobelin fusion protein with ZZ-domain of S. aureus protein A in E. coil by recombinant DNA techniques. The pro2Z-obelin expressed was purified by one-step affinity chromatography on IgG-Agarose. The purified proZZ-obelin has both the luminescent activity of obelin and the IgG-binding ability of ZZ-domain. The specific activity of fusion protein was 8.5 x 10(15) photons per mg of protein. (C) 1996 Academic Press, Inc.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Petushkov V.N., Gibson B.G., Lee J.
Заглавие : The yellow bioluminescence bacterium, Vibrio fischeri Y1, contains a bioluminescence active riboflavin protein in addition to the yellow fluorescence FMN protein
Место публикации : Biochemical and Biophysical Research Communications. - 1995. - Vol. 211, Is. 3. - С. 774-779. - ISSN 0006291X (ISSN) , DOI 10.1006/bbrc.1995.1880
Ключевые слова (''Своб.индексиров.''): riboflavin--article--bioluminescence--fluorescence--nonhuman--priority journal--protein analysis--protein synthesis--vibrio--vibrionaceae--bacterial proteins--chromatography, gel--chromatography, thin layer--flavin mononucleotide--flavoproteins--luminescence--riboflavin--spectrometry, fluorescence--support, u.s. gov't, p.h.s.--vibrio--bacteria (microorganisms)--photobacterium--vibrio--vibrio fischeri
Аннотация: The yellow bioluminescence Y1 strain of Vibrio fischeri can produce a 22 kDa protein with either FMN or riboflavin as a bound fluorophore. Both forms are active for shifting the bioluminescence spectral maximum. The fluorescence spectral distribution of the two proteins differs slightly and the in vivo emission appears to be an equal mixture of the two. The bioluminescence activity of the riboflavin Y1 protein contrasts with the inactivity of the related Photobacterium type.
Scopus
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Makhutova O.N., Sushchik N.N., Kalacheva G.S.
Заглавие : The value of fatty acid composition of tricylglycerols and polar lipids of seston at analysis of food spectra of microzooplancton in small reservoir Buguch
Место публикации : Doklady Akademii Nauk. - 2004. - Vol. 395, Is. 4. - С. 562-565. - ISSN 08695652 (ISSN)
Ключевые слова (''Своб.индексиров.''): algae--bacteria--chromatographic analysis--chromatography--organic compounds--food spectra--microzooplancton--polar lipids--microorganisms
Аннотация: Food spectrum of microzooplancton in fresh-water ecological systems is lowly studied area. However, these organisms play very important role in transfer of substance and energy in water reservoirs. Traditional method of analysis of food in the microzooplancton does not makes it possible to determine real assimilation of organic substance. Therefore, biochemical methods have been developed which are based on analysis of compositions of fatty acids of organic substance. This leads to determining of the food assimilation. Fatty-acid compositions of lipids allow specialists to determine specific groups of organisms such as bacteria, microalgae etc. Data of the analysis are presented.
Scopus
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Petushkov V.N., Rodionova N.S., Bondar' V.S.
Заглавие : Study of the luminescence system of the soil enchytraeid Fridericia heliota (Annelida: Clitellata: Oligochaeta: Enchytraeidae)
Место публикации : Doklady Biochemistry and Biophysics. - 2003. - Vol. 391, Is. 1-6. - С. 204-207. - ISSN 16076729 (ISSN) , DOI 10.1023/A:1025105323648
Ключевые слова (''Своб.индексиров.''): adsorption chromatography--animal cell--annelid worm--article--luminescence--nonhuman--purification--animal--drug antagonism--isolation and purification--metabolism--physiology--soil--animalia--annelida--clitellata--enchytraeidae--edetic acid--luciferase--magnesium--animals--edetic acid--luciferases--luminescent measurements--magnesium--oligochaeta--soil
Scopus
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Chang D., Liu Y., Chen Y., Hu X., Burov A., Puzyr A., Bondar V., Yao L.
Заглавие : Study of the immunogenicity of the VP2 protein of canine parvovirus produced using an improved Baculovirus expression system
Место публикации : BMC Vet. Res.: BioMed Central Ltd., 2020. - Vol. 16, Is. 1. - Ст.202. - ISSN 17466148 (ISSN), DOI 10.1186/s12917-020-02422-3
Аннотация: Background: Canine parvovirus (CPV) is now recognized as a serious threat to the dog breeding industry worldwide. Currently used CPV vaccines all have their specific drawbacks, prompting a search for alternative safe and effective vaccination strategies such as subunit vaccine. VP2 protein is the major antigen targeted for developing CPV subunit vaccine, however, its production in baculovirus expression system remains challenging due to the insufficient yield. Therefore, our study aims to increase the VP2 protein production by using an improved baculovirus expression system and to evaluate the immunogenicity of the purified VP2 protein in mice. Results: The results showed that high-level expression of the full length VP2 protein was achieved using our modified baculovirus expression system. The recombinant virus carrying two copies of VP2 gene showed the highest expression level, with a productivity of 186 mg/L, which is about 1.4-1.6 fold that of the recombinant viruses carrying only one copy. The purified protein reacted with Mouse anti-His tag monoclonal antibody and Rabbit anti-VP2 polyclonal antibody. BALB/c mice were intramuscularly immunized with purified VP2 protein twice at 2 week intervals. After vaccination, VP2 protein could induce the mice produce high level of hemagglutination inhibition antibodies. Conclusions: Full length CPV VP2 protein was expressed at high level and purified efficiently. Moreover, it stimulated mice to produce high level of antibodies with hemmaglutination inhibition properties. The VP2 protein expressed in this study could be used as a putative economic and efficient subunit vaccine against CPV infection. © 2020 The Author(s).
Scopus
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Kudryavtsev A.N., Krasitskaya V.V., Petunin A.I., Burakov A.Y., Frank L.A.
Заглавие : Simultaneous Bioluminescent Immunoassay of Serum Total and IgG-Bound Prolactins
Колич.характеристики :6 с
Место публикации : Anal. Chem.: AMER CHEMICAL SOC, 2012. - Vol. 84, Is. 7. - С. 3119-3124. - ISSN 0003-2700, DOI 10.1021/ac300444w
Примечания : Cited References: 10. - This work was supported in part by Grant No. 76 of the Russian Academy of Sciences, Siberian Branch and by the Program of the Government of Russian Federation "Measures to attract leading scientists to Russian educational institutions" (Grant No 11. G34.31.058).
Предметные рубрики: PHOTOPROTEIN OBELIN
POLYETHYLENE-GLYCOL
MACROPROLACTINEMIA
PRECIPITATION
VALIDATION
Аннотация: Novel dual-analyte single-well bioluminescence immunoassay (BLIA) for total and IgG-bound prolactins was developed on the base of Ca2+-regulated photoprotein obelin mutants with altered color and kinetics of bioluminescence signal as reporters. The mutants W92F-H22E and Y138F were chemically conjugated with monoclonal mouse anti-hPRL and anti-hIgG immunoglobulins and thus displayed signals from total prolactin and IgG-bounded prolactin (macroprolactin) correspondingly. Bioluminescence of the reporters was simultaneously triggered by a single injection of Ca2+ solution and discriminated via bioluminescent signal spectral and time resolution. The developed microplate-based immunoassay allows detection of two prolactin forms in crude serum without additional manipulations (e.g., gel chromatography or PEG-precipitation). Total prolactin bioluminescence immunoassay in standard, control, and clinical sera offers high sensitivity and reproducibility. The BLIA results show good correlation with those obtained by RIA and immunoassay after gel chromatography.
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Kalacheva G.S., Sushchik N.N., Gladyshev M.I., Makhutova O.N.
Заглавие : Seasonal dynamics of fatty acids in the lipids of water moss Fontinalis antipyretica from the Yenisei River
Место публикации : Russian Journal of Plant Physiology. - 2009. - Vol. 56, Is. 6. - С. 795-807. - ISSN 10214437 (ISSN) , DOI 10.1134/S1021443709060090
Ключевые слова (''Своб.индексиров.''): acetylenic acids--fatty acids--fontinalis antipyretica--seasonal dynamics--bryophyta--fontinalis antipyretica
Аннотация: Identification of lipid fatty acids (FA) and studying of their seasonal dynamics in water moss Fontinalis antipyretica from the Yenisei River were carried out by means of gas chromatography-mass spectrometry. FA composition of water moss was notable for a relatively low level of saturated acids and predominance of polyunsaturated acids (PUFA) with double bonds (accounting for more than 30% of total FA) and polyunsaturated acids with double and triple bonds (acetylenic acids, accounting for more than 40% of total FA). Among PUFA, ?- and ?-linolenic (18:3?3 and 18:3?6), arachidonic (20:4?6), and eicosapentaenoic (20:5?3) acids prevailed. Relative content of PUFA from ?3-family was the greatest in spring, and the level of PUFA from ?6-group was essentially the same throughout all the seasons. In the biomass of water moss, we identified seven acetylenic acids; among them octadeca-9,12-dien-6-ynoic (6a,9,12-18:3), octadeca-9,12,15-trien-6-ynoic (6a,9,12,15-18:4), and eicosa-11,14-dien-8-ynoic (8a,11,14-20:3) acids were predominant. For the first time, in the lipids of water moss we identified an acetylenic eicosa-11,14,17-trien-8-ynoic acid (8a,11,14,15-20:4). Relative content of acetylenic acids in the total FA was great throughout the entire period of investigation with the peak accumulation in summer. Owing to a steadily high level in the biomass of water moss and the lack of other producers of these acids in the ecosystem, acetylenic FA are highly specific biochemical markers useful for the investigation of trophic interactions between higher aquatic plants and zoobenthos. В© Pleiades Publishing, Ltd., 2009.
Scopus
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Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Sushchik N.N., Gladyshev M.I., Kalachova G.S., Guseynova V.E.
Заглавие : Rapid assay of fatty acid composition using a portable high-performance liquid chromatograph for monitoring aquatic ecosystems
Место публикации : Journal of Chromatography A. - 1995. - Vol. 695, Is. 2. - С. 223-228. - ISSN 00219673 (ISSN) , DOI 10.1016/0021-9673(94)01090-2
Ключевые слова (''Своб.индексиров.''): fatty acid--alga--article--culture medium--ecology--high performance liquid chromatography--instrument--methodology--priority journal--ultraviolet spectrophotometry--water analysis
Аннотация: The chromatographic conditions presented allowed the separation of the nitrophenacyl derivatives of standards of eleven free fatty acids (FFA) using a portable high-performance chromatograph, suitable for use aboard a research vessel. A statistically significant linear correlation between UV absorbance and amount of the analytes injected was obtained. The method was tested on FFA from algae cultural media. The method can be used for the ecological monitoring of natural waters.
Scopus
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10.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Petushkov V.N., Rodionova N.S.
Заглавие : Purification and partial spectral characterization of a novel luciferin from the luminous enchytraeid Fridericia heliota
Место публикации : Journal of Photochemistry and Photobiology B: Biology. - 2007. - Vol. 87, Is. 2. - С. 130-136. - ISSN 10111344 (ISSN) , DOI 10.1016/j.jphotobiol.2007.03.006
Ключевые слова (''Своб.индексиров.''): atp--bioluminescence--earthworms--enchytraeid--luciferase--luciferin--adenosine triphosphate--luciferase--luciferin--animal cell--anion exchange chromatography--annelid worm--article--controlled study--earthworm--firefly--luminance--luminescence--nonhuman--priority journal--protein analysis--protein purification--radiation absorption--reversed phase liquid chromatography--ultraviolet radiation--adenosine triphosphate--animals--luciferases--luminescent agents--oligochaeta--spectrum analysis--enchytraeidae--fridericia heliota
Аннотация: A homogeneous luciferin preparation has been obtained from the luminous soil enchytraeid Fridericia heliota, which has an ATP-dependent luminescent system. A procedure for luciferin purification without losing fractions of active luciferase has been developed. The luciferin specific activity is 4000 times increased; its UV absorption spectrum maximum is 294 nm with a local minimum at 262 nm. The luciferin of the enchytraeid F. heliota is significantly different from firefly luciferin, whose luminescent reaction also requires ATP, and it also appears to have no similarities to other known luciferins. В© 2007 Elsevier B.V. All rights reserved.
Scopus
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11.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Sevastianov V.I., Perova N.V., Shishatskaya E.I., Kalacheva G.S., Volova T.G.
Заглавие : Production of purified polyhydroxyalkanoates (PHAs) for applications in contact with blood
Место публикации : Journal of Biomaterials Science, Polymer Edition. - 2003. - Vol. 14, Is. 10. - С. 1029-1042. - ISSN 09205063 (ISSN) , DOI 10.1163/156856203769231547
Ключевые слова (''Своб.индексиров.''): ?-hydroxy acids--endotoxins--hemocompatibility--poly(hydroxybutyrate-co-hydroxyvalerate) (phbv)--polyhydroxyalkanoates (phas)--polyhydroxybutyrate (phb)--bacterium lipopolysaccharide--carbon--complement--copolymer--hydroxyacid--long chain fatty acid--poly(3 hydroxybutyric acid)--polyhydroxyalkanoic acid--valeric acid derivative--adult--article--biofilm--biotechnology--blood analysis--blood clotting--blood compatibility--cell function--chemical analysis--chemical composition--complement activation--concentration (parameters)--controlled study--gas chromatography--hemostasis--human--human cell--mass spectrometry--micromorphology--nonhuman--priority journal--purification--quantitative analysis--sampling--synthesis--thrombocyte adhesion--wautersia eutropha--biocompatible materials--blood--blood coagulation tests--chromatography, gas--complement activation--cupriavidus necator--fatty acids--humans--platelet adhesiveness--polyesters--surface properties
Аннотация: Samples of olyhydroxyalkanoates (PHAs), polyhydroxybutyrate (PHB) and copolymers poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) with 4 and 18 mol% hydroxyvalerate, synthesized by the bacteria Ralstonia eutropha B5786, were investigated. PHA films in contact with blood did not activate the hemostasis system at the level of cell response, but they did activate the coagulation system and the complement reaction. To detect biologically-active components in the PHAs, a detailed analysis of the composition of the polymers was conducted. Gas chromatography-mass spectrometry revealed long-chain fatty acids (FAs) in the tested PHAs. Their total concentration in the polymer ranged from tenths of mol% to 2-3 mol%, depending on the purification method. C16:0 constituted the largest proportion, up to 70%. Of the long-chain hydroxy acids, only ?-OH-C14:0 was detected and it did not exceed 0.06 mol%. The analysis of the hemocompatibility properties of the PHAs purified by a specialized procedure, including the quantitative and morphological estimation of platelets adherent to the surface of polymer films, the plasma recalcification time and complement activation studies, indicated that PHB and PHBV can be used in contact with blood. It has been found out that the lipopolysaccharides of bacteria producing PHAs, which contain mostly long-chain hydroxy acids, can be the factor activating the hemostasis systems. Thus, the technology of PHA purification must satisfy rather stringent specific requirements.
Scopus
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12.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Sevastianov V.I., Perova N.V., Shishatskaya E.I., Kalacheva G.S., Volova T.G.
Заглавие : Production of purified polyhydroxyalkanoates (PHAs) for applications in contact with blood
Колич.характеристики :14 с
Место публикации : J. Biomater. Sci.-Polym. Ed.: VSP BV, 2003. - Vol. 14, Is. 10. - P1029-1042. - ISSN 0920-5063, DOI 10.1163/156856203769231547
Примечания : Cited References: 34
Предметные рубрики: BIODEGRADABLE POLYESTERS
POLYMERS
Ключевые слова (''Своб.индексиров.''): polyhydroxyalkanoates (phas)--polyhydroxybutyrate (phb)--poly(hydroxybutyrate-co-hydroxyvalerate) (phbv)--endotoxins--beta-hydroxy acids--hemocompatibility
Аннотация: Samples of olyhydroxyalkanoates (PHAs), polyhydroxybutyrate (PHB) and copolymers poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) with 4 and 18 mol% hydroxyvalerate, synthesized by the bacteria Ralstonia eutropha B5786, were investigated. PHA films in contact with blood did not activate the hemostasis system at the level of cell response, but they did activate the coagulation system and the complement reaction. To detect biologically-active components in the PHAs, a detailed analysis of the composition of the polymers was conducted. Gas chromatography-mass spectrometry revealed long-chain fatty acids (FAs) in the tested PHAs. Their total concentration in the polymer ranged from tenths of mol% to 2-3 mol%, depending on the purification method. C-16:0 constituted the largest proportion, up to 70%. Of the long-chain hydroxy acids, only beta-OH-C-14:0 was detected and it did not exceed 0.06 mol%. The analysis of the hemocompatibility properties of the PHAs purified by a specialized procedure, including the quantitative and morphological estimation of platelets adherent to the surface of polymer films, the plasma recalcification time and complement activation studies, indicated that PHB and PHBV can be used in contact with blood. It has been found out that the lipopolysaccharides of bacteria producing PHAs, which contain mostly long-chain hydroxy acids, can be the factor activating the hemostasis systems. Thus, the technology of PHA purification must satisfy rather stringent specific requirements.
WOS
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13.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : BONDAR V.S., TROFIMOV K.P., VYSOTSKII E.S.
Заглавие : PHYSICOCHEMICAL PROPERTIES OF A PHOTOPROTEIN FROM THE HYDROID POLYP OBELIA-LONGISSIMA
Место публикации : Biochem.-Moscow: PLENUM PUBL CORP, 1992. - Vol. 57, Is. 10. - С. 1020-1027. - 8. - ISSN 0006-2979
Примечания : Cited References: 36
Предметные рубрики: CALCIUM-ACTIVATED PHOTOPROTEINS
CTENOPHORES MNEMIOPSIS SP
BEROE-OVATA
AEQUORIN
CA-2+
INDICATORS
PROTEIN
BINDING
PURIFICATION
EXTRACTION
Ключевые слова (''Своб.индексиров.''): bioluminescence--ca2+-activated photoprotein--obelin--chromatography--calcium
Аннотация: The photoprotein obelin was isolated and purified to homogeneity (as indicated by sodium dodecyl sulfate polyacrylamide gel electrophoresis) from hydroids of Obelia longissima by gel filtration on Sephadex G-75 fine, ion exchange chromatography on Polysil CA-300 (10 mum), hydrophobic chromatography on Phenyl-Sepharose CL-4B, gel filtration on Sephacryl S-200 superfine, ion exchange chromatography on a Mono Q column at pH 7.0, chromatofocusing on a Mono P column (pH gradient 6.0-4.0), and ion exchange chromatography on a Mono Q column at pH 5.5, 8.8, and 7.0. The molecular weight of the native protein was 30 kD, and that measured in the presence of SDS was 19.8 kD. The specific activity of obelin is 4.9.10(15) quanta/mg protein, pseudo-first-order constant of bioluminescence decay 4 sec-1, and quantum yield 0.16 The range of measurable Ca2+ concentrations is 10(-7) to 10(-5) M. The luminescence spectrum of obelin peaks at 469 nm, and the fluorescence emission maximum of the discharged protein is at 455 nm. The optimum pH for luminescence is between 9.0 and 10.5. The molecular ionization constants are pK1 6.8 and pK2 12.2, and the ionization constants for the active site are pK1 9.1 and pK2 10.2
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14.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Purtov K.V., Puzyr A.P., Bondar V.S.
Заглавие : Nanodiamond sorbents: New carriers for column chromatography of proteins
Колич.характеристики :3 с
Место публикации : Dokl. Biochem. Biophys.: SPRINGER, 2008. - Vol. 419, Is. 1. - С. 72-74. - ISSN 1607-6729, DOI 10.1134/S1607672908020075
Примечания : Cited References: 12
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15.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Gladyshev, Michail I., Sushchik, Nadezhda N., Tolomeev, Alexander P., Dgebuadze, Yury Yu
Заглавие : Meta-analysis of factors associated with omega-3 fatty acid contents of wild fish
Колич.характеристики :23 с
Коллективы : Russian Science Foundation [16-14-10001]
Место публикации : Rev. Fish. Biol. Fish.: SPRINGER, 2018. - Vol. 28, Is. 2. - С. 277-299. - ISSN 0960-3166, DOI 10.1007/s11160-017-9511-0. - ISSN 1573-5184(eISSN)
Примечания : Cited References:138. - The work was supported by a Russian Science Foundation Grant (No. 16-14-10001).
Предметные рубрики: FATTY-ACID-COMPOSITION
DIETARY DOCOSAHEXAENOIC ACID
LONG-CHAIN
Ключевые слова (''Своб.индексиров.''): docosahexaenoic acid--ecomorphological factors--eicosapentaenoic acid--nutritive value--phylogenetic factors
Аннотация: Fish are recognized as the main source of physiologically important omega-3 long-chain polyunsaturated fatty acids, namely, eicosapentaenoic acid (EPA) and docosahexaenoic acid (DHA), for human nutrition. However, muscle tissue contents of these fatty acids in diverse fish species, i.e., their nutritive value for humans, varied within two orders of magnitude. We reviewed contents of EPA and DHA, measured by similar methods using an internal standard during chromatography as mg per g of wet mass in 172 fish species belonging to 16 orders, to evaluate probable variations in phylogenetic and ecological drivers. EPA + DHA content varied from 25.6 mg g(-1) of wet mass (Sardinops sagax) to 0.12 mg g(-1) (Gymnura spp.). Multidimensional redundancy analysis revealed that among phylogenetic, ecomorphological and abiotic environmental factors, the highest proportion of variation contribution belonged to the shared contribution of sets of phylogenetic and ecomorphological factors. Specifically, the highest values of EPA + DHA content were characteristic of fish belonging to the orders Clupeiformes or Salmoniformes, were pelagic fast swimmers, ate zooplankton and inhabited marine waters or migrated from fresh to marine waters (anadromous migrations). High EPA and DHA content in muscle tissues of the above species appeared to be a metabolic adaptation for fast continuous swimming. In contrast to common beliefs, our meta-analysis did not support the significant influence of higher trophic levels (piscivory) and cold environments (homeoviscous adaptation) on EPA and DHA content in fish. However, many causes of high and low levels of physiologically important fatty acids in certain fish species remained unexplained and require evaluation in future studies.
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16.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Marques S.M., Petushkov V.N., Rodionova N.S., Esteves Da Silva J.C.G.
Заглавие : LC-MS and microscale NMR analysis of luciferin-related compounds from the bioluminescent earthworm Fridericia heliota
Место публикации : Journal of Photochemistry and Photobiology B: Biology. - 2011. - Vol. 102, Is. 3. - С. 218-223. - ISSN 10111344 (ISSN) , DOI 10.1016/j.jphotobiol.2010.12.006
Ключевые слова (''Своб.индексиров.''): bioluminescence--earthworm--fridericia heliota--luciferin--microscale nmr--rp-hplc-ms--alkene--alkyl group--benzothiazole--carboxylic acid--hydroxyl group--luciferin--pterin--absorption--article--bioluminescence--earthworm--fridericia heliota--isomer--molecular weight--nonhuman--nuclear magnetic resonance--priority journal--reversed phase high performance liquid chromatography--ultraviolet radiation--animals--chromatography, high pressure liquid--chromatography, reverse-phase--firefly luciferin--luminescent agents--magnetic resonance spectroscopy--mass spectrometry--oligochaeta--fridericia heliota
Аннотация: This paper presents the main results of RP-HPLC-MS and microscale NMR analysis performed on Accompanying similar to Luciferin (AsLn(x)), compounds present in extracts of the bioluminescent earthworm Fridericia heliota that display similarities with Fridericia's luciferin, the substrate of the bioluminescent reaction. Three isomers of AsLn were discovered, AsLn(1), AsLn(2) and AsLn(3), all of which present a molecular weight of 529 Da. Their UV-Vis absorption spectra show maxima at 235 nm for AsLn(1), 238 and 295 nm for AsLn(2) and 241 and 295 nm for AsLn(3). MS n fragmentation patterns suggest the existence of carboxylic acid and hydroxyl moieties, and possibly chemical groups found in other luciferins like pterin or benzothiazole. The major isomer, AsLn(2), presents an aromatic ring and alkene and alkyl moieties. These luciferin-like compounds can be used as models that could give further insights into the structure of this newly discovered luciferin. В© 2010 Elsevier Inc. All rights reserved.
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17.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Kuznetsov, Boris N., Malyar, Yuriy N., Kuznetsova, Svetlana A., Grishechko, Lyudmila I., Kazachenko, Alexander S., Levdansky, Alexander V., Pestunov, Andrey V., Boyandin, Anatoly N., Celzard, Alan
Заглавие : Isolation, Study and Application of Organosolv Lignins
Колич.характеристики :29 с
Место публикации : J. Sib. Fed. Univ.-Chem.: SIBERIAN FEDERAL UNIV, 2016. - Vol. 9, Is. 4. - С. 454-482. - ISSN 1998-2836, DOI 10.17516/1998-2836-2016-9-4-454-482. - ISSN 2313-6049(eISSN)
Примечания : Cited References:137
Предметные рубрики: SIZE-EXCLUSION CHROMATOGRAPHY
MOLECULAR-WEIGHT DISTRIBUTION
Ключевые слова (''Своб.индексиров.''): organosolv lignin--isolation--structure--catalytic depolymerization--molecular weight--application--liquid hydrocarbons--aerogels
Аннотация: The analysis of the literature on the methods of soluble organosolv lignins isolation, their physical-chemical study and on the method of their processing to porous aerogels and liquid hydrocarbons was carried out. A review of the literature allowed us to choice of the most important areas of research. For isolation from wood the soluble lignins free from sulfur the methods of catalytic peroxide delignification at mild conditions (temperature
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18.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Eke G..., Kuzmina A.M., Goreva A.V., Shishatskaya E.I., Hasirci N..., Hasirci V...
Заглавие : In vitro and transdermal penetration of PHBV micro/nanoparticles
Колич.характеристики :11 с
Коллективы : Government of the Russian Federation [220, 11.G34.31.0013, MD-3112.2012.4]; EC FP7 SKINTREAT project; State Planning Organization (Turkey)
Место публикации : J. Mater. Sci.-Mater. Med.: SPRINGER, 2014. - Vol. 25, Is. 6. - С. 1471-1481. - ISSN 0957-4530, DOI 10.1007/s10856-014-5169-5. - ISSN 1573-4838
Примечания : Cited References: 38. - The study was supported by the Government of the Russian Federation (Decree No. 220 of 09.04.2010) (Agreement No. 11.G34.31.0013) and (Grant No MD-3112.2012.4). We gratefully acknowledge the EC FP7 SKINTREAT project and the State Planning Organization (Turkey) for the grant to establish BIOMATEN. Mr. A. Buyuksungur is acknowledged for his contributions with CLSM.
Предметные рубрики: DRUG-DELIVERY
PLGA NANOPARTICLES
CELLULAR UPTAKE
MICROPARTICLES
POLYHYDROXYALKANOATES
CYTOTOXICITY
SIZE
POLYESTERS
MECHANISM
CELLS
Аннотация: The purpose of this study was to develop micro and nano sized drug carriers from poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV), and study the cell and skin penetration of these particles. PHBV micro/nanospheres were prepared by o/w emulsion method and were stained with a fluorescent dye, Nile Red. The particles were fractionated by centrifugation to produce different sized populations. Topography was studied by SEM and average particle size and its distribution were determined with particle sizer. Cell viability assay (MTT) was carried out using L929 fibroblastic cell line, and particle penetration into the cells were studied. Transdermal permeation of PHBV micro/nanospheres and tissue reaction were studied using a BALB/c mouse model. Skin response was evaluated histologically and amount of PHBV in skin was determined by gas chromatography-mass spectrometry. The average diameters of the PHBV micro/nanosphere batches were found to be 1.9 mu m, 426 and 166 nm. Polydispersity indices showed that the size distribution of micro sized particles was broader than the smaller ones. In vitro studies showed that the cells had a normal growth trend. MTT showed no signs of particle toxicity. The 426 and 166 nm sized PHBV spheres were seen to penetrate the cell membrane. The histological sections revealed no adverse effects. In view of this data nano and micro sized PHBV particles appeared to have potential to serve as topical and transdermal drug delivery carriers for use on aged or damaged skin or in cases of skin diseases such as psoriasis, and may even be used in gene transfer to cells.
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19.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Ronzhin N. O., Mogilnaya O. A., Artemenko K. S., Posokhina E. D., Bondar V. S.
Заглавие : Extracellular Oxidases of Basidiomycete Neonothopanus nambi: Isolation and Some Properties
Колич.характеристики :5 с
Место публикации : Dokl. Biochem. Biophys.: MAIK NAUKA/INTERPERIODICA/SPRINGER, 2020. - Vol. 490, Is. 1. - С. 38-42. - ISSN 1607-6729, DOI 10.1134/S1607672920010135. - ISSN 1608-3091(eISSN)
Примечания : Cited References:15
Предметные рубрики: PEROXIDASE-ACTIVITY
LIGHT-EMISSION
Аннотация: Using the original technique of treating biomass with beta-glucosidase, a pool of extracellular fungal enzymes was obtained for the first time from the mycelium of basidiomycete Neonothopanus nambi. Two protein fractions containing enzymes with oxidase activity were isolated from the extract by gel-filtration chromatography and conventionally called F1 and F2. Enzyme F1 has a native molecular weight of 80-85 kDa and does not contain chromophore components; however, it catalyzes the oxidation of veratryl alcohol with K-m = 0.52 mM. Probably, this enzyme is an alcohol oxidase. Enzyme F2 with a native molecular weight of approximately 60 kDa is a FAD-containing protein. It catalyzes the cooxidation of phenol with 4-aminoantipyrine without the addition of exogenous hydrogen peroxide, which distinguishes it from the known peroxidases. It was assumed that this enzyme may be a mixed-function oxidase. F2 oxidase has K-m value 0.27 mM for phenol. The temperature optimums for oxidases F1 and F2 are 22-35 and 55-70 degrees C, and pH optimums are 6 and 5, respectively.
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20.

Вид документа : Статья из журнала
Шифр издания :
Автор(ы) : Mogilnaya, Olga, Ronzhin, Nikita, Posokhina, Ekaterina, Bondar, Vladimir
Заглавие : Extracellular Oxidase from the Neonothopanus nambi Fungus as a Promising Enzyme for Analytical Applications
Колич.характеристики :10 с
Коллективы : [0356-2019-0022]
Место публикации : Protein J.: SPRINGER, 2021. - Article in press. - ISSN 1572-3887, DOI 10.1007/s10930-021-10010-z. - ISSN 1573-4943(eISSN)
Примечания : Cited References:39. - This work was supported by the state budget allocated to the fundamental research at the Russian Academy of Sciences, Project No. 0356-2019-0022.
Предметные рубрики: ARYL-ALCOHOL OXIDASE
GLUCOSE-OXIDASE
PEROXIDASES
MECHANISM
Аннотация: The extracellular enzyme with oxidase function was extracted from the Neonothopanus nambi luminescent fungus by using mild processing of mycelium with beta-glucosidase and then isolated by gel-filtration chromatography. The extracted enzyme is found to be a FAD-containing protein, catalyzing phenol co-oxidation with 4-aminoantipyrine without addition of H2O2, which distinguishes it from peroxidases. This fact allowed us to assume that this enzyme may be a mixed-function oxidase. According to gel-filtration chromatography and SDS-PAGE, the oxidase has molecular weight of 60 kDa. The enzyme exhibits maximum activity at 55-70 degrees C and pH 5.0. Kinetic parameters K-m and V-max of the oxidase for phenol were 0.21 mM and 0.40 mu M min(-1). We suggest that the extracted enzyme can be useful to develop a simplified biosensor for colorimetric detection of phenol in aqueous media, which does not require using hydrogen peroxide.
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